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Clinical and Diagnostic Laboratory Immunology, September 1999, p. 734-740, Vol. 6, No. 5
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

A New Sensitive Serological Assay for Detection of Lentivirus Infections in Small Ruminants

Eric Saman,1,* Geertrui Van Eynde,1 Luis Lujan,2 Belén Extramiana,3 Gordon Harkiss,4 Francesco Tolari,5 Lorenzo Gonzàlez,3,dagger Beatriz Amorena,6 Neil Watt,4 and Juan Badiola2

Innogenetics NV, B-9052 Zwijnaarde, Belgium1; Department of Animal Pathology, University of Zaragoza, 50013 Zaragoza,2 Instituto Vasco de Investigación y Desarrollo Agrario, 48160 Derio,3 and Servicio de Investigación Agroalimentaria, SIA-DGA, 50008 Zaragoza,6 Spain; Department of Veterinary Pathology, University of Edinburgh, EH29 9RG Edinburgh, United Kingdom4; and Department of Animal Pathology, University of Pisa, 56124 Pisa, Italy5

Received 6 May 1999/Returned for modification 15 June 1999/Accepted 9 July 1999

Lentivirus infections in small ruminants represent an economic problem affecting several European countries with important sheep-breeding industries. Programs for control and eradication of these infections are being initiated and require reliable screening assays. This communication describes the construction and evaluation of a new serological screening enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies to maedi-visna virus (MVV) in sheep and to caprine arthritis encephalitis virus (CAEV) in goats. The solid phase is sensitized with a combination of the major core protein p25 of MVV produced in Escherichia coli and a peptide derived from the immunodominant region of the viral transmembrane protein gp46. The peptide carries an N-terminal biotin residue and is complexed with streptavidin prior to being coated. The new assay was evaluated with 2,336 sheep serum samples from different European countries with large differences in the levels of prevalence of MVV infections, and the results have been compared to those of the standard agar gel immunodiffusion test. Discrepant samples were analyzed by Western blotting with viral lysate, and most sera could be classified unambiguously. The estimated overall sensitivity of the new ELISA was 99.4% (95% confidence interval [CI], 98.4 to 99.8%) and the specificity was 99.3% (95% CI, 98.7 to 99.6%). A limited set of goat sera (n = 212) was also analyzed, with similar results. These data indicate that the new assay is a reliable tool that can be used in control and eradication programs for small ruminant lentivirus infections.


* Corresponding author. Mailing address: Innogenetics NV, Industriepark 7/4, B-9052 Zwijnaarde, Belgium. Phone: 32/9 241 0783. Fax: 32/9 241 0907. E-mail: ericsam{at}innogenetics.be.

dagger Present address: The Moredun Research Institute, Pentland Science Park, Penicuik, United Kingdom.


Clinical and Diagnostic Laboratory Immunology, September 1999, p. 734-740, Vol. 6, No. 5
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



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